JP2017036282A5 - - Google Patents

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JP2017036282A5
JP2017036282A5 JP2016164314A JP2016164314A JP2017036282A5 JP 2017036282 A5 JP2017036282 A5 JP 2017036282A5 JP 2016164314 A JP2016164314 A JP 2016164314A JP 2016164314 A JP2016164314 A JP 2016164314A JP 2017036282 A5 JP2017036282 A5 JP 2017036282A5
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adhesive
chlorhexidine salt
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chlorhexidine
adhesives
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別な特徴では、本発明はクロルヘキシジンを含有する接着剤の作成方法を提供する。この方法は、少なくとも一つのクロルヘキシジン塩の水溶液を提供するステップと、その水溶液を積極的に乾燥させることでその少なくとも一つの固体形状であるクロルヘキシジン塩を得るステップとを含んでいる。この方法は、接着剤成分を提供するステップと、その接着剤成分と相溶性の溶媒を提供するステップとをさらに含んでいる。この方法は、クロルヘキシジン溶液を作成するため、その溶媒内でその固体形状のクロルヘキシジンを溶解させるステップをさらに含んでいる。さらに、この方法はそのクロルヘキシジン溶液をその接着剤成分と組み合わせることでクロルヘキシジン含有接着剤を作成するステップをさらに含んでいる。 In another aspect, the present invention provides a method for making an adhesive containing a chlorhexidine salt . The method includes providing an aqueous solution of at least one chlorhexidine salt, and actively drying the aqueous solution to obtain the chlorhexidine salt in its at least one solid form. The method further includes providing an adhesive component and providing a solvent compatible with the adhesive component. The method further includes dissolving the solid form of the chlorhexidine salt in the solvent to create a chlorhexidine salt solution. The method further includes the step of making the chlorhexidine- containing adhesive by combining the chlorhexidine salt solution with the adhesive component.

本発明は、クロルヘキシジングルコネートを、医療用および外科的利用において幅広く利用されている溶媒ベースのアクリル接着剤などの溶媒ベースの接着剤へ含有させるための独特な手法を提供する。この新規な方法では、好適には、粉末を得るためにクロルヘキシジングルコネートのフリーズドライ処理またはスプレードライ処理による積極乾燥法によってクロルヘキシジングルコネートを溶媒ベースの接着剤へと含有させる。この粉末はその後にアクリル接着剤などの対象接着剤と相溶性の溶媒中に溶解される。典型的なアクリル接着剤のための適切な溶媒の1例はメタノールである。

The present invention provides a unique approach for incorporating chlorhexidine gluconate into solvent-based adhesives such as solvent-based acrylic adhesives that are widely used in medical and surgical applications. In this novel process, chlorhexidine gluconate is preferably incorporated into the solvent-based adhesive by a freeze-drying or spray drying process of chlorhexidine gluconate to obtain a powder. This powder is then dissolved in a solvent compatible with the target adhesive, such as an acrylic adhesive. One example of a suitable solvent for a typical acrylic adhesive is methanol.

Claims (33)

少なくとも一つのクロルヘキシジン塩の水溶液を準備するステップと、
前記水溶液を積極乾燥させることで前記少なくとも一つの固体形状のクロルヘキシジン塩を得るステップと、
接着剤成分を準備するステップと、
前記接着剤成分と相溶性の溶媒を準備するステップと、
前記溶媒内で固体形状のクロルヘキシジンを溶解させてクロルヘキシジン溶液を作成するステップと、
前記クロルヘキシジン溶液を前記接着剤成分と組み合わせることでクロルヘキシジン塩含有接着剤を作成するステップと、
を含む、クロルヘキシジンを含有する接着剤の作成方法。
Providing an aqueous solution of at least one chlorhexidine salt;
Obtaining the at least one solid form of chlorhexidine salt by actively drying the aqueous solution;
Preparing an adhesive component;
Providing a solvent compatible with the adhesive component;
Dissolving a solid form of chlorhexidine salt in the solvent to create a chlorhexidine salt solution;
Creating a chlorhexidine salt-containing adhesive by combining the chlorhexidine salt solution with the adhesive component;
A method for producing an adhesive containing a chlorhexidine salt .
前記水溶液は1重量%〜前記少なくとも一つのクロルヘキシジン塩の溶解限度までの総濃度の前記少なくとも一つのクロルヘキシジン塩を含む、請求項1記載の方法。 The method of claim 1 , wherein the aqueous solution comprises a total concentration of the at least one chlorhexidine salt from 1% by weight to the solubility limit of the at least one chlorhexidine salt. 前記少なくとも一つのクロルヘキシジン塩は、クロルヘキシジンジグルコネートを含む、請求項1または2記載の方法。   The method of claim 1 or 2, wherein the at least one chlorhexidine salt comprises chlorhexidine digluconate. 前記水溶液中のクロルヘキシジンジグルコネートの濃度は20重量%または40重量%のいずれかである、請求項3記載の方法。 The concentration of chlorhexidine digluconate in the aqueous solution is either 20% or 40% by weight, The method of claim 3. 前記積極乾燥はフリーズドライ法またはスプレードライ法のいずれかを含む、請求項1から4のいずれかに記載の方法。   The method according to claim 1, wherein the aggressive drying includes either a freeze drying method or a spray drying method. 前記フリーズドライ法−80℃10℃の範囲内の温度で実施される、請求項5記載の方法。 The method according to claim 5, wherein the freeze-drying method is performed at a temperature in the range of -80 ° C to 10 ° C. 前記温度−50℃である、請求項6記載の方法。 The method according to claim 6, wherein the temperature is −50 ° C. to 0 ° C. 前記温度−20℃である、請求項7記載の方法。 The method of claim 7, wherein the temperature is −20 ° C. 前記フリーズドライ法0.01バール〜0.95バールの範囲内の圧力で実施される、請求項5記載の方法。 The method of claim 5, wherein the freeze-drying method is performed at a pressure in the range of 0.01 bar to 0.95 bar. 前記圧力0.10バール0.50バールである、請求項9記載の方法。 The method of claim 9, wherein the pressure is between 0.10 bar and 0.50 bar. 前記圧力0.18バールである、請求項10記載の方法。 The method of claim 10, wherein the pressure is 0.18 bar. 前記固体形状は粒子形態である、請求項1記載の方法。   The method of claim 1, wherein the solid form is a particulate form. 前記フリーズドライ法は、少なくとも一つのクロルヘキシジン塩の水溶液をスプレー処理することを含む、請求項5記載の方法。   6. The method of claim 5, wherein the freeze drying method comprises spraying an aqueous solution of at least one chlorhexidine salt. 前記接着剤成分は、(i)接着剤成分、(ii)接着剤プレミックス、および(iii)接着剤処方物から成る群から選択される、請求項1記載の方法。   The method of claim 1, wherein the adhesive component is selected from the group consisting of (i) an adhesive component, (ii) an adhesive premix, and (iii) an adhesive formulation. 前記接着剤成分は接着剤処方物である、請求項14記載の方法。 The method of claim 14 , wherein the adhesive component is an adhesive formulation. 前記接着剤処方物はアクリル接着剤、ゴム接着剤、シリコン接着剤、ポリウレタン接着剤およびこれらの組み合わせから成る群から選択される、請求項15記載の方法。 The method of claim 15 , wherein the adhesive formulation is selected from the group consisting of acrylic adhesives, rubber adhesives, silicone adhesives, polyurethane adhesives, and combinations thereof. 前記接着剤処方物はアクリル接着剤を含む、請求項15記載の方法。 The method of claim 15 , wherein the adhesive formulation comprises an acrylic adhesive. 前記溶媒はメタノールである、請求項1〜17のいずれかに記載の方法。 The solvent is methanol The method of any of claims 1-17. 請求項1〜18のいずれかに記載の方法によって製造された、少なくとも一つのクロルヘキシジンを含有する接着剤処方物Produced by the process according to any one of claims 1 to 18 adhesive formulation containing at least one chlorhexidine salt. 前記接着剤は、アクリル接着剤、ゴム接着剤、シリコン接着剤、ポリウレタン接着剤およびこれらの組み合わせから成る群から選択される、請求項19記載の処方物。 20. The formulation of claim 19 , wherein the adhesive is selected from the group consisting of acrylic adhesives, rubber adhesives, silicone adhesives, polyurethane adhesives, and combinations thereof. 前記接着剤はアクリル接着剤である、請求項19記載の処方物。 20. The formulation of claim 19 , wherein the adhesive is an acrylic adhesive. 前記少なくとも一つのクロルヘキシジン塩は、クロルヘキシジンジグルコネートを含む、請求項1921のいずれか1項に記載の処方物。 The formulation according to any one of claims 19 to 21 , wherein the at least one chlorhexidine salt comprises chlorhexidine digluconate. 前記クロルヘキシジン塩は粉末形態であり、積極乾燥処理によって製造される、請求項1922のいずれか1項に記載の処方物。 23. A formulation according to any one of claims 19 to 22 , wherein the chlorhexidine salt is in powder form and is produced by aggressive drying. 前記積極乾燥処理はフリーズドライ法である、請求項23記載の処方物。 24. The formulation of claim 23 , wherein the aggressive drying process is a freeze drying process. 前記積極乾燥処理はスプレードライ法である、請求項23記載の処方物。 24. The formulation of claim 23 , wherein the aggressive drying process is a spray drying method. 抗菌特性を備えた接着剤を有する医療用製品であって、請求項1〜18のいずれか1項に記載の方法により製造された接着剤含む、医療用製品。 A medical article having an adhesive having antimicrobial properties, including an adhesive manufactured by the method according to any one of claims 1 to 18, a medical product. 前記接着剤処方物は、
接着剤、および
少なくとも一つのクロルヘキシジン塩を含む、請求項26記載の医療用製品。
The adhesive formulation is:
27. The medical product of claim 26 , comprising an adhesive and at least one chlorhexidine salt.
前記接着剤は、アクリル接着剤、ゴム接着剤、シリコン接着剤、ポリウレタン接着剤およびこれらの組み合わせから成る群から選択される、請求項27記載の医療用製品。 28. The medical product of claim 27 , wherein the adhesive is selected from the group consisting of acrylic adhesives, rubber adhesives, silicone adhesives, polyurethane adhesives, and combinations thereof. 前記接着剤はアクリル接着剤である、請求項28記載の医療用製品。 30. The medical product of claim 28 , wherein the adhesive is an acrylic adhesive. 前記少なくとも一つのクロルヘキシジン塩は、クロルヘキシジングルコネートを含む、請求項27記載の医療用製品。 28. The medical product of claim 27 , wherein the at least one chlorhexidine salt comprises chlorhexidine gluconate. 前記クロルヘキシジン塩は粉末形態であり、積極乾燥処理によって製造される、請求項2730のいずれか1項に記載の医療用製品。 The medical product according to any one of claims 27 to 30 , wherein the chlorhexidine salt is in a powder form and is produced by a positive drying process. 前記積極乾燥処理はフリーズドライ法である、請求項31記載の医療用製品。 32. The medical product according to claim 31 , wherein the aggressive drying treatment is a freeze drying method. 前記積極乾燥処理はスプレードライ法である、請求項31記載の医療用製品。 32. The medical product according to claim 31 , wherein the aggressive drying process is a spray drying method.
JP2016164314A 2011-01-21 2016-08-25 Chlorhexidine gluconate-containing solvent adhesive Active JP6280175B2 (en)

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US201161434991P 2011-01-21 2011-01-21
US61/434,991 2011-01-21

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EP (1) EP2665363B1 (en)
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CN (2) CN103442572A (en)
BR (1) BR112013018616B1 (en)
DK (1) DK2665363T3 (en)
ES (1) ES2767278T3 (en)
HK (1) HK1246213A1 (en)
HU (1) HUE048016T2 (en)
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